FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Unifi Workspace v1.0.0

K Number: K190694 · Decision Jul 11, 2019
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
32
Review Days
115

Basic Information

Device Name
Unifi Workspace v1.0.0
K Number
K190694
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hologic, Inc.
Date Received
March 18, 2019
Decision Date
July 11, 2019
Product Code
LLZ
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LLZ System, Image Processing, Radiological

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